EP2962951B1 - Plaque métallique stratifiée pour canettes en deux parties et corps de stratifiée en deux parties - Google Patents

Plaque métallique stratifiée pour canettes en deux parties et corps de stratifiée en deux parties Download PDF

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Publication number
EP2962951B1
EP2962951B1 EP13876472.5A EP13876472A EP2962951B1 EP 2962951 B1 EP2962951 B1 EP 2962951B1 EP 13876472 A EP13876472 A EP 13876472A EP 2962951 B1 EP2962951 B1 EP 2962951B1
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EP
European Patent Office
Prior art keywords
polyester resin
metal sheet
film
resin layer
pet
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EP13876472.5A
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German (de)
English (en)
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EP2962951A1 (fr
EP2962951A4 (fr
Inventor
Yusuke Nakagawa
Junichi Kitagawa
Yoichiro Yamanaka
Yoichi Tobiyama
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JFE Steel Corp
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JFE Steel Corp
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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00—Layered products having a non-planar shape
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D7/00—Containers having bodies formed by interconnecting or uniting two or more rigid, or substantially rigid, components made wholly or mainly of metal
    • B65D7/02—Containers having bodies formed by interconnecting or uniting two or more rigid, or substantially rigid, components made wholly or mainly of metal characterised by shape
    • B65D7/04—Containers having bodies formed by interconnecting or uniting two or more rigid, or substantially rigid, components made wholly or mainly of metal characterised by shape of curved cross-section, e.g. cans of circular or elliptical cross-section
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00—Layered products having a non-planar shape
    • B32B1/08—Tubular products
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B32B15/09—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/14—Linings or internal coatings
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/03—3 layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/40—Symmetrical or sandwich layers, e.g. ABA, ABCBA, ABCCBA
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B32B2307/536—Hardness
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles
    • B32B2439/40—Closed containers
    • B32B2439/66—Cans, tins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles
    • B32B2439/70—Food packaging

Definitions

  • the present invention relates to a laminated metal sheet for a two-piece can and a two-piece laminated can body.
  • Metal cans as one form of food packaging containers are excellent in mechanical strength and long-term preservability, can be packed with high-temperature contents as they are and can be hermetically sealed, can be easily subjected to sterilization treatment such as retort sterilization treatment after the hermetic sealing, and are thus highly safe and hygienic as packaging containers.
  • Metal cans have the advantage that they are easily separated and collected from wastes.
  • Metal cans have been conventionally manufactured from coated metal sheets, in which coating processes performed in can manufacturers are, however, complicated and low in productivity.
  • a solvent-based coating material when a solvent-based coating material is used, a large amount of solvents volatilizes in drying and baking treatment performed after coating, and environmental problems such as discharge of solvents occur.
  • BPA bisphenol A
  • laminated metal sheets with a BPA-free thermoplastic resin film thermally fusion-bonded to a metal sheet surface have been used as a metal can material.
  • Laminated metal sheets with a polyester resin film thermally fusion-bonded to a metal sheet surface in particular are excellent in performance in terms of food sanitation and are thus widely used.
  • the laminated metal sheets with a polyester resin film thermally fusion-bonded to a metal surface are used for lids, drawn and redrawn (DRD) cans, drawn and ironed (DI) cans, or the like.
  • Patent Literature 1 and Patent Literature 2 disclose a technique in which a biaxially oriented polyethylene terephthalate film is laminated onto a metal sheet through an adhesive layer formed of a low melting point polyester, which is used as a metal can material.
  • US20140339123 discloses a laminated metal sheet comprising a metal sheet; a first polyester resin layer formed on a surface of the metal sheet that serves as an exterior of a container after being formed into the container; and a second polyester resin layer formed on another surface of the metal sheet that serves as an interior of the container after being formed into the container, wherein the first polyester resin layer contains not less than 30% by mass and not more than 60% by mass of polyethylene terephthalate or copolymerized polyethylene terephthalate having a copolymerization component content of less than 6 mol %, and not less than 40% by mass and not more than 70% by mass of polybutylene terephthalate, the second polyester resin layer is copolymerized polyethylene terephthalate having a copolymerization component content of less than 14 mol %, and the first and the second polyester resin layers have a degree of residual orientation of not less than 2% and not more than 50%, and have thicknesses after lamination of not less than 6 ⁇ m. Wax may be applied
  • Patent Literature 3 and Patent Literature 4 disclose a method that manufactures a laminated metal sheet and a metal can body with a high drawing ratio using a thermally fusion-bondable polyester resin film.
  • the laminated metal sheet that is thermally fusion-bonded with a polyester resin film is used on the outer face side of a food canned container, that is, the side being in contact with high-temperature vapor during the retort sterilization treatment, the retort sterilization treatment causes a retort whitening phenomenon, which changes the color of the polyester resin film and impairs design. For this reason, when the laminated metal sheet that is thermally fusion-bonded with a polyester resin film is used on the outer face side of the food canned container, the laminated metal sheet is required to have retort whitening resistance.
  • the laminated metal sheet that is thermally fusion-bonded with a polyester resin film is used on the inner face side of the food canned container, the laminated metal sheet is required to have corrosion resistance.
  • the laminated metal sheet is required to have mechanical properties that enable forming with a high degree of processing such as "drawing” and "drawing and ironing”.
  • Patent Literature 5 describes that increasing a crystallization rate of a polymer can suppress the retort whitening phenomenon, the mechanism of the retort whitening phenomenon is not completely determined, and the problem of the retort whitening phenomenon is not completely solved.
  • Patent Literatures 6 to 9 describe metal-sheet covering films for use in drawing and ironing by laminating a film formed of butylene terephthalate and ethylene terephthalate onto a metal sheet.
  • a flat laminated metal sheet is insufficient in processability for use in containers such as food canned containers and may cause defects such as breakage of the film.
  • a steel sheet which has higher strength than that of an aluminum sheet, is used as a base material in particular, damage occurs in the film during formation, and the steel sheet cannot be used as a can body.
  • the present invention has been made in view of the above problems, and an object thereof is to provide a laminated metal sheet for a two-piece can having retort whitening resistance and corrosion resistance and having mechanical properties that enable forming with a high degree of processing and a two-piece laminated can body manufactured by using the laminated metal sheet for a two-piece can.
  • a laminated metal sheet for a two-piece can includes: a metal sheet; a first polyester resin layer formed on a surface of the metal sheet, the surface forming an outer face side of a container after container formation; and a second polyester resin layer formed on a surface of the metal sheet, the surface forming an inner face side of the container after container formation.
  • the first polyester resin layer contains polyethylene terephthalate or a copolymerized polyethylene terephthalate with a content of a copolymerized component of less than 6 mol% in a ratio of 30% to 60% by mass, polybutylene terephthalate or a copolymerized polybutylene terephthalate with a content of a copolymerized component of less than 5 mol% in a ratio of 40% to 70% by mass, and a polyolefinic wax in an amount of 0.01% to 3.0% in outer percentage, the second polyester resin layer is a copolymerized polyethylene terephthalate with a content of a copolymerized component of less than 22 mol%, and residual degrees of orientation of the first and the second polyester resin layers are less than 30%.
  • a center line surface roughness Ra of a surface of the first polyester resin layer is within a range of 0.4 ⁇ m to 2.0 ⁇ m.
  • a two-piece laminated can body according to the present invention is manufactured by using the laminated metal sheet for a two-piece can according to the present invention.
  • the present invention can provide a laminated metal sheet for a two-piece can having retort whitening resistance and corrosion resistance and having mechanical properties that enable forming with a high degree of processing and a two-piece laminated can body manufactured by using the laminated metal sheet for a two-piece can.
  • the laminated metal sheet for a two-piece includes a metal sheet, an outer face side polyester resin layer formed on a surface of the metal sheet, the surface forming an outer face side of a container after container formation, and an inner face side polyester resin layer formed on a surface of the metal sheet, the surface forming an inner face side of the container after container formation.
  • a steel sheet or an aluminum sheet widely used as can materials can be used, and particularly preferable is tin free steel (TFS), which is a surface-treated steel sheet having a two-layer film in which the lower layer and the upper layer are formed of metal chromium and chromium hydroxide, respectively.
  • TFS tin free steel
  • adhesion amounts of metal chromium and chromium hydroxide of the TFS include, but are not limited to, within the range of 70 mg/m 2 to 200 mg/m 2 for the adhesion amount of metal chromium and within the range of 10 mg/m 2 to 30 mg/m 2 for the adhesion amount of chromium hydroxide from the viewpoint of processability and corrosion resistance.
  • the can body packed with the contents is exposed to high-temperature, high-pressure vapor immediately after the start of the retort sterilization treatment.
  • part of the vapor passes through the polyester resin film and goes near the surface of the metal sheet.
  • the can body packed with the contents is cooled by the contents packed before the retort sterilization treatment, and the polyester resin film near the surface of the metal sheet is lower in temperature than that of an ambient atmosphere.
  • the water vapor is cooled within the amorphous polyester resin film near the metal sheet to be condensed to water.
  • the condensed water extends the polyester resin film to form water bubbles.
  • these water bubbles are vaporized by a temperature increase of the contents, and the vaporized water bubbles transform into the voids.
  • the polyester resin film near the metal sheet is cooled by the contents and is thermally fusion-bonded, and the film becomes an amorphous layer, in which crystal orientation breaks down.
  • the mechanical strength of the polyester resin film near the metal sheet is lower than that of a crystalline layer and is easily deformed. This fact is considered to cause the above phenomenon. Consequently, the retort whitening phenomenon can be suppressed if the strength of the amorphous layer near the metal sheet can be increased.
  • manufacture is performed by heating the metal sheet to a high temperature not less than a glass transition point and fusion-bonding the polyester resin film thereonto, and the resin layer near the surface of the metal sheet is fused, by which an oriented crystal inevitably breaks down. Given these circumstances, the present invention makes the amorphous layer, which is low in mechanical strength and fragile immediately after lamination, a hard, strong layer after being formed into a can body, thereby suppressing the retort whitening phenomenon.
  • Examples of a method for crystalizing the polyester resin film as the amorphous layer before the retort sterilization treatment include a method that performs heat treatment before the retort sterilization treatment.
  • Concerning a case of performing the heat treatment before container formation a polyester resin film having high crystal orientation is inferior in formability and is thus limited in the form of cans for which the method can be used, which is not realistic.
  • a case of performing the heat treatment after container formation has the disadvantage that an increase in post-formation processes increases manufacturing costs.
  • the inventors of the present invention aiming at increasing crystal orientation by utilizing heat during the retort sterilization treatment, have found a resin composition having a high thermal crystallization rate and have used the resin composition for the outer face side polyester resin layer.
  • the present invention crystallizes the polyester resin as the amorphous layer before the voids are formed in the resin layer on the can outer face through the retort sterilization treatment and increases strength.
  • a specific, effective composition for increasing the thermal crystallization rate of a first polyester resin layer formed on a surface of the metal sheet, the surface forming the outer face side of a container after container formation is a polyester composition obtained by mixing a polyester (hereinafter, may be written as a polyester (A)) with polyethylene terephthalate as a main component and a polyester (hereinafter, may be written as a polyester (B)) with polybutylene terephthalate as a main component, the ratio of the polyester (A) being 60% by mass or less and the ratio of the polyester (B) being 40% by mass or more.
  • the ratio of the polyester (A) exceeds 60% by mass and the ratio of the polyester (B) is less than 40% by mass, the formation of voids near the surface of the metal sheet cannot be suppressed during the retort sterilization treatment, and the resin layer whitens to impair design significantly.
  • the ratio of the polyester (A) is less than 30% by mass and the ratio of the polyester (B) exceeds 70% by mass, although the retort whitening phenomenon can be suppressed, the modulus of elasticity of the resin layer excessively decreases to impair mechanical properties, and flaws easily occur in the resin layer during transport or during forming, and suitability for food canned containers is difficult. In addition, the price is too high from the viewpoint of resin cost, which is thus not suitable for practical use.
  • the ratio in mass% (A/B) between the polyester (A) and the polyester (B) is preferably in the range of 30 to 60/70 to 40 and more preferably in the range of 40 to 50/60 to 50.
  • the polyester (A) is obtained by a melt condensation reaction with a terephthalic acid component and an ethylene glycol component as main components.
  • Another component may be copolymerized with polyethylene terephthalate in an amount of less than 6 mol% as a range that does not impair the effects of the present invention, and the copolymerized component may be an acid component or an alcohol component.
  • the copolymerized component examples include aromatic dicarboxylic acids such as isophthalic acid, phthalic acid, and naphthalene dicarboxylic acid; aliphatic dicarboxylic acids such as adipic acid, azelaic acid, sebacic acid, and decane dicarboxylic acid; and alicyclic dicarboxylic acids such as cyclohexane dicarboxylic acid.
  • aromatic dicarboxylic acids such as isophthalic acid, phthalic acid, and naphthalene dicarboxylic acid
  • aliphatic dicarboxylic acids such as adipic acid, azelaic acid, sebacic acid, and decane dicarboxylic acid
  • alicyclic dicarboxylic acids such as cyclohexane dicarboxylic acid.
  • isophthalic acid is particularly preferable.
  • the copolymerized alcohol component examples include aliphatic diols such as butanediol and hexanediol and alicyclic diols such as cyclohexane dimethanol. They may be used singly, or two or more of them may be used.
  • the ratio of the copolymerized component is, depending on its type, a ratio so as to give a resulting polymer melting point within the range of 210°C to 256°C, preferably 215°C to 256°C, and more preferably 220°C to 256°C. If the polymer melting point is less than 210°C, heat resistance is poor. If the polymer melting point exceeds 256°C, the crystallinity of the polymer is too high, and forming processability is impaired.
  • the polyester (B) is obtained by a melt condensation reaction with a terephthalic acid component and a 1,4-butanediol component as main components.
  • Another component may be copolymerized in an amount of less than 5 mol% as a range that does not impair the effects of the present invention, and the copolymerized component may be an acid component or an alcohol component.
  • Examples of the copolymerized acid component include aliphatic dicarboxylic acids such as isophthalic acid, phthalic acid, and naphthalene dicarboxylic acid; aliphatic dicarboxylic acids such as adipic acid, azelaic acid, sebacic acid, and decane dicarboxylic acid; and aliphatic dicarboxylic acids such as cyclohexane dicarboxylic acid.
  • isophthalic acid or 2,6-naphthalene dicarboxylic acid is preferable.
  • the copolymerized alcohol component examples include aliphatic diols such as ethylene glycol and hexane diol and alicyclic diols such as cyclohexane dimethanol. They can be used singly, or two or more of them can be used.
  • the ratio of the copolymerized component is, depending on its type, a ratio so as to give a resulting polymer melting point within the range of 180°C to 223°C, preferably 200°C to 223°C, and more preferably 210°C to 223°C. If the polymer melting point is less than 180°C, crystallinity as polyester is low, resulting in poor heat resistance.
  • the mixing ratio between the polyester (A) and the polyester (B) is adjusted so that the polymer melting point is within the range of 200°C to 256°C, more preferably 210°C to 256°C, and more preferably 220°C to 256°C.
  • Examples of an olefinic wax to be added include homopolymers and copolymers of olefins, copolymers of olefins and other copolymerizable monomers such as a vinyl monomer, and modified copolymers thereof.
  • polyethylenes high density, low density low molecular weight, high molecular weight, or the like
  • linear low density polyethylenes linear ultra-low density polyethylenes
  • polypropylenes ethylene-propylene copolymers
  • poly-4-methylene-pentene-1 ionomer resins
  • ethylene-vinyl acetate copolymers ethylene-acrylic acid copolymers
  • ethylene-methyl methacrylate copolymers ethylene-methyl methacrylate copolymers
  • modified polyolefins reaction products of homopolymers, copolymers, or the like of olefins and unsaturated carboxylic acids such as maleic acid and fumaric acid, acid anhydrides, esters, metallic salts, or the like.
  • These olefins can be used singly, or two or more of them can be used mixedly.
  • a low molecular weight wax with a number-average molecular weight (Mn) of 1,000 to 10,000 is effective and preferred.
  • Mn number-average molecular weight
  • the content of the olefinic wax is within the range of 0.01% or more and 3.0% or less in terms of a mass ratio to the outer face side polyester resin layer. If the content is less than 0.01%, a less amount of the olefinic wax appears on the resin surface, and processability is poor. If the content exceeds 3.0%, the effect of increasing processability is nearly saturated, followed by technical obstacles in manufacturing and reduction in productivity, leading to an excessive cost increase.
  • the olefinic wax is added in an amount within the range of 0.01% or more and 3.0% or less in outer percentage and preferably in an amount within the range of 0.01% or more and 1.0% or less in outer percentage.
  • a center line surface roughness Ra of the surface of the outer face side polyester resin layer is preferably 0.4 ⁇ m or more and 2.0 ⁇ m or less.
  • Containers such as beverage cans are generally required to have high luster, and the surface of laminated metal sheets for use in such containers is kept smooth.
  • Films for use in such high-luster laminated metal sheets generally have a surface roughness Ra of 0.1 ⁇ m or less, and even after lamination the film surface smoothness is kept to have a surface roughness of about 0.1 ⁇ m.
  • Such smooth laminated metal sheets are likely to cause defects in the film by drawing and ironing or to reduce adhesion with a base material and thus cannot be used for food cans under severe use conditions.
  • the lower limit of the surface roughness is 0.4 ⁇ m or more. If the surface roughness exceeds 2.0 ⁇ m, film thickness becomes uneven, and film defects or the like easily occur. For this reason, the upper limit of the surface roughness is 2.0 ⁇ m or less and more preferably 1.5 ⁇ m or less.
  • a polyester (a polyester (C)) with polyethylene terephthalate as a main component is formed.
  • the polyethylene (C) is a polymer formed of a dicarboxylic acid component with terephthalic acid as a main component and a glycol component with ethylene glycol as a main component.
  • the dicarboxylic acid component include terephthalic acid, isophthalic acid, naphthalene dicarboxylic acid, and diphenyl dicarboxylic acid. Among these, terephthalic acid or isophthalic acid is preferably used.
  • the glycol component may contain propanediol, butanediol, or the like with ethylene glycol as the main component.
  • the main component is polyethylene terephthalate and may copolymerize, with a content of a compolymerized component being less than 22 mol%.
  • the content is preferably less than 18 mol% and more preferably less than 15 mol%. If the content of the copolymerized component is 22 mol% or more, the melting point decreases too much, and residual degrees of orientation of the outer face side and the inner face side polyester resin layers cannot be adjusted to be within a certain range when laminated, resulting in no effect.
  • the ratio of the copolymerized component is, depending on its type, a ratio so as to give a resulting polymer melting point within the range of 210°C to 256°C, preferably 215°C to 256°C, and more preferably 220°C to 256°C. If the polymer melting point is less than 210°C, heat resistance is poor. If the polymer melting point exceeds 256°C, the crystallinity of the polymer is too high, and forming processability is impaired. Antioxidants, heat stabilizers, UV absorbers, plasticizers, pigments, antistatic agents, crystal nucleating agents, or the like may be added as needed.
  • the above-described inner face side polyester resin layer is excellent in mechanical properties such as tensile strength, the modulus of elasticity, and impact strength and further has polarity, and the inner face side polyester resin layer as the main component can increase the adhesion and formability of the inner face side polyester resin layer up to a level that can withstand container processing and impart impact resistance after the container processing.
  • An important characteristic of a polyethylene terephthalate laminate film is that an amount of oriented crystals has a large influence on characteristics.
  • the amount of oriented crystals is controlled to an appropriate amount in accordance with required performance by taking advantage of this characteristic, thereby separately producing laminated metal sheets having desired basic performance.
  • laminate conditions in the thermal fusion-bonding method are precisely controlled, and a residual amount of oriented crystals is controlled.
  • the present invention in accordance with a degree of processing required for the use as two-piece cans, controls the residual degree of orientation of a biaxial oriented polyester resin film to be within the range of less than 30%.
  • the residual degree of orientation is a value determined by the X-ray diffraction method and is defined as follows.
  • the residual degrees of orientation of the outer face side polyester resin layer and the inner face side polyester resin layer are less than 30%. If the residual degree of orientation is 30% or more, film formability is poor, and body breakage occurs during the manufacture of cans, or problems such as film delamination occur after processing.
  • a biaxially stretched polyester film is thermally fusion-bonded, the oriented crystals break down by heat from the metal sheet, and the resin layer changes into an amorphous polyester resin. If heat input is small during thermal fusion-bonding, the resin layer is insufficiently fused on the interface with the metal sheet, and the adhesion between the metal sheet and the resin layer is poor.
  • the adhesion of the resin layer required when used for food canned containers be ensured and that formability be ensured by reducing the residual degree of orientation to a certain level or less and increasing the ratio of the amorphous polyester resin layer excellent in deformability laminated onto the metal sheet. Consequently, it is necessary that the residual degrees of orientation of the outer face side polyester resin layer and the inner face side polyester resin layer be less than 30% and preferably in the range of 20% or less. From the viewpoint of film formability, it is desirable that, in accordance with a higher degree of processing, the residual degree of orientation be reduced as much as possible. Although no specific lower limit of the residual degree of orientation is set, the residual degree of orientation is preferably 2% or more, because if the residual degree of orientation is less than 2%, impact resistance tends to be poor.
  • the outer face side polyester resin layer preferably contains polyethylene terephthalate or a copolymerized polyethylene terephthalate obtained by copolymerizing preferably isophthalic acid as an acid component in a ratio of less than 6 mol% as needed
  • the inner face side polyester resin layer preferably contains a copolymerized polyethylene terephthalate obtained by copolymerizing preferably isophthalic acid as an acid component in a ratio of less than 22 mol%.
  • the inner face side polyester resin layer is used on the inner face side of a can, and it is copolymerized in order to ensure adhesion.
  • the outer face side polyester resin layer and the inner face side polyester resin layer are after container formation on the outer face side and the inner face side, respectively, and are required to have the above-described necessary characteristics.
  • the residual degree of orientation is determined so as to exhibit the required characteristics. If the ratios of the amorphous polyester are significantly different between the inner face and the outer face when laminated, the necessary characteristics cannot be satisfied on one side or both sides. In such a case, manufacture with the target residual degrees of orientation satisfying the necessary characteristics of both sides simultaneously is difficult.
  • the outer face side polyester resin layer and the inner face side polyester resin layer are preferably adjusted in composition so that their residual degrees of orientation are not significantly departed from each other.
  • the temperature of the metal sheet and the melting point of the resin when laminated have close relation, and the temperature of the metal sheet is determined by the resin melting point.
  • the resin melting point depends on the resin composition; polybutylene terephthalate has a lower melting point than that of polyethylene terephthalate, and the melting point significantly changes depending on the mixing ratio. Isophthalic acid-copolymerized polyethylene terephthalate has a lower melting point than that of polyethylene terephthalate.
  • the resin melting point of the outer face side polyester resin layer can be sufficiently reduced compared with the resin melting point of the inner face side polyester resin layer, and polyethylene terephthalate that is not copolymerized can be used for the outer face side polyester resin layer.
  • the polyester (A) can be compolymerized with isophthalic acid to adjust the resin melting point.
  • the thicknesses of the outer face side polyester resin layer and the inner face side polyester resin layer when flaws occur by rubbing or the like during formation or when food canned containers are transported, the surface of the metal sheet may be exposed to impair appearance, or corrosion may occur with the exposed part of the metal sheet as a starting point during long-term storage.
  • the thicknesses of the outer face side polyester resin layer and the inner face side polyester resin layer are preferably 10 ⁇ m or more and 40 ⁇ m or less. If the thicknesses are less than 10 ⁇ m, corrosion resistance may not be ensured. If the thicknesses exceed 40 ⁇ m, an excessive cost increase in manufacture is brought about.
  • the respective polyester resins are dried as needed, and one of them and/or each of them is supplied to a known melt lamination extruder, is extruded in a sheet shape from a slit-shaped die, is brought into intimate contact with a casting drum by a process of static electricity application or the like, and is cooled and solidified to be a non-stretched sheet.
  • the non-stretched sheet is then stretched in the longitudinal direction and the width direction of the film to obtain a biaxially stretched film.
  • a stretch ratio can be freely set in accordance with the degree of orientation, the strength, the modulus of elasticity, or the like of a target film.
  • the method for manufacturing is preferably a tenter process in view of film quality, and preferably a successive biaxial stretch process including a stretch in the longitudinal direction followed by a stretch in the width direction and a simultaneous biaxial stretch process including nearly simultaneous stretches in the longitudinal direction and the width direction.
  • Examples of a method for manufacturing the laminated metal sheet include, but are not limited to, a method that heats a metal sheet at a temperature exceeding the melting point of a film, brings resin films into contact with both sides thereof, and thermally fusion-bonds the resin films thereonto using pressure rolls (hereinafter referred to as laminate rolls).
  • Laminate conditions are appropriately set so that resin layers prescribed by the present invention can be obtained.
  • the temperature of the metal sheet during lamination is preferably 160°C or more, and a contact time at the melting point of the film or more is preferably in the range of 1 msec to 20 msec as a temperature history that the film undergoes during lamination.
  • the pressure as a surface pressure is preferably from 0.098 MPa to 2.94 MPa (from 1 kgf/cm 2 to 30 kgf/cm 2 ). If the surface pressure is too low, even if the temperature of the interface of the resin reaches a temperature at or higher than the melting point, the time is short, and sufficient adhesion cannot be obtained. If the surface pressure is high, although there is no inconvenience on the performance of the laminated metal sheet, force acting on the laminate rolls is large, and strength in terms of equipment is required, which leads to an increase in the size of an apparatus and is thus uneconomical.
  • degreasing, pickling, and chromium plating treatment were performed on a steel sheet with a thickness of 0.20 mm subjected to cold rolling, annealing, and temper rolling to produce a chromium-plated steel sheets (TFS).
  • chromium plating treatment the chromium plating treatment is performed with a chromium plating bath containing CrO 3 , F - , and SO 4 2- , and after intermediate rinsing, electrolysis was performed with a chemical conversion treatment liquid containing CrO 3 and F - .
  • electrolysis conditions current density, quantity of electricity, or the like
  • adhesion amounts of metal chromium and chromium hydroxide were 120 mg/m 2 and 15 mg/m 2 in terms of Cr, respectively.
  • the chromium-plated steel sheet was heated using a metal sheet covering apparatus, and resin films of Inventive Examples 1 to 25 and Comparative Examples 1 to 11 listed in Table 1 below were laminated through thermal fusion-bonding so that the outer face side polyester resin layer (an outer face side resin layer) and the inner face side polyester resin layer (an inner face side resin layer) are formed on one and the other sides, respectively, of the chromium-plated steel sheet by the laminate rolls to manufacture a laminated metal sheet.
  • the laminate rolls are of an internal water-cooling type, and cooling water was forcedly circulated during lamination to perform cooling during film adhesion. Characteristics of the laminated steel sheet and the films on the laminated steel sheet were evaluated by the following methods.
  • PET and PET/I in Table 1 represent polyethylene terephthalate and isophthalic acid-copolymerized polyethylene terephthalate, respectively.
  • a paraffin wax with a melting point of 45°C was applied to both sides of the laminated steel sheet in an amount of 50 mg/m 2 , and a blank with a diameter of 123 mm was punched out therefrom.
  • the blank was drawn and formed into a cup with an inner diameter of 71 mm and a height of 36 mm by a commercially available cupping press.
  • the cup was then charged into a commercial DI forming apparatus, and by redrawing and three-stage ironing with a punch speed of 200 mm/s and a stroke of 560 mm, a total reduction rate of 50% (with reduction rates of the respective steps of 30%, 19%, and 23%) was achieved to finally form a can with a can inner diameter of 52 mm and a can height of 90 mm.
  • tap water was circulated at a temperature of 50°C.
  • the residual degree of crystal orientation is a value determined by the X-ray diffraction method and is defined as follows.
  • the center line surface roughness Ra was measured in conformity with JIS-B0601 using a surface roughness measuring instrument SE-30D manufactured by Kosaka Laboratory Ltd. with a cut-off value of 0.8 mm and a measurement length of 2.4 mm. Measurement was performed at respective three points in the longitudinal direction and the width direction of a film, and the average value of the Ra values was determined to be the Ra value of the film.
  • Drawing and ironing formability was evaluated based on the presence or absence of body breakage after forming by marking an example in which body breakage occurred after drawing and ironing with D and marking an example manufacturable as a can with A.
  • the following evaluations (2) to (5) were performed on only samples manufacturable as a can.
  • Outer face coverability was evaluated by the soundness of a can outer face film after forming (an example with less defects is favorable). Specifically, for a drawn and ironed can after being washed and dried, a scratch was made on a can mouth by a file so that a current could be passed through the steel sheet of the drawn and ironed can, and the drawn and ironed can was put in a container (slightly larger than the drawn and ironed can) containing an electrolytic solution (a 1% NaCl solution with a temperature of 25°C) with the base of the drawn and ironed can directed downward so that only the outer face of the can was in contact with the electrolytic solution. Subsequently, the outer face coverability was evaluated based on a current value measured when a voltage of 6 V was applied across the can body and the electrolytic solution in accordance with the following criteria.
  • a resin-laminated steel sheet was drawn and ironed to produce a can, in which water was packed as contents and a lid was seamed. Subsequently, the can was placed in a retort sterilization furnace with the can bottom directed downward, and the retort sterilization treatment was performed at 125°C for 90 minutes. After the treatment, changes in the appearance of the can bottom were visually observed in accordance with the following criteria.
  • a can was filled with tap water at room temperature, and a lid was seamed to hermetically seal the can.
  • Ten cans were dropped onto a polyvinyl chloride floor from a height of 1.25 m for each test, and the lid and the tap water within the can were removed. A spot of the film on the upper end part of the can was cut away to expose the steel sheet.
  • the can was then filled with a 5% salt solution.
  • a platinum electrode was inserted into the solution (the position inserted was the center of the can) as a cathode, with the upper end part of the can (the steel sheet exposed part) as an anode. Subsequently, a voltage of 6 V was applied across the platinum electrode and the can, and a current value after a lapse of 3 seconds was read. An average value after measuring the ten cans was calculated, and the impact resistance was evaluated based on the average value in accordance with the following criteria.
  • the laminated steel sheets of Inventive Examples 1 to 25 have all of the drawing and ironing formability, the outer face coverability, the outer face retort whitening resistance, the inner face corrosion resistance, and the inner face impact resistance.
  • the laminated steel sheets of Comparative Examples 1 to 11 are inferior in any of the drawing and ironing formability, the outer face coverability, the outer face retort whitening resistance, the inner face corrosion resistance, and the inner face impact resistance.
  • the laminated steel sheets of Inventive Examples 1 to 25 can provide a laminated steel sheet having retort whitening resistance and corrosion resistance and having mechanical properties that enable forming with a high degree of processing such as drawing and drawing and ironing.
  • the present invention can provide a laminated metal sheet for a two-piece can having retort whitening resistance and corrosion resistance and having mechanical properties that enable forming with a high degree of processing and a two-piece laminated can body manufactured by using the laminated metal sheet for a two-piece can.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Rigid Containers With Two Or More Constituent Elements (AREA)
  • Wrappers (AREA)

Claims (3)

  1. Tôle métallique stratifiée pour une boîte de conserve en deux parties, la tôle métallique stratifiée comprenant :
    une tôle métallique ;
    une première couche de résine polyester formée sur une surface de la tôle métallique, la surface formant un côté de face extérieure d'un récipient après formation de récipient ; et
    une seconde couche de résine polyester formée sur une surface de la tôle métallique, la surface formant un côté de face intérieure du récipient après formation de récipient, dans laquelle
    la première couche de résine de polyester contient du polyéthylène téréphtalate ou un polyéthylène téréphtalate copolymérisé ayant une teneur en composant copolymérisé inférieure à 6 % en mole selon un rapport de 30 % à 60 % en masse, du polybutylène téréphtalate ou un polybutylène téréphtalate copolymérisé ayant une teneur en composant copolymérisé inférieure à 5 % en mole selon un rapport de 40 % à 70 % en masse, et une cire polyoléfinique selon une quantité de 0,01 % à 3,0 % en pourcentage extérieur,
    la seconde couche de résine de polyester est un polyéthylène téréphtalate copolymérisé ayant une teneur en composant copolymérisé inférieure à 22 % en mole, et
    des degrés d'orientation résiduels des première et seconde couches de résine de polyester sont inférieurs à 30 %, le degré résiduel d'orientation cristalline étant une valeur déterminée par le procédé de diffraction des rayons X et étant défini de la manière suivante : (1) pour une résine de polyester orientée (ou un film de polyester orienté) avant stratification et la résine (ou le film) après stratification, une intensité de diffraction des rayons X est mesurée dans la plage de 2θ = 20° à 30° ; (2) les valeurs d'intensité de diffraction des rayons X à 2θ = 20° et à 2θ = 30° sont reliées par une ligne droite, qui est définie comme une ligne de base; (3) la hauteur du pic le plus élevé apparaissant à proximité de 2θ = de 22° à 28° est mesurée à partir de la ligne de base ; (4) P2/P1 x 100 est défini comme un degré d'orientation résiduel (%), P1 étant la hauteur du pic le plus élevé du film avant stratification, et P2 étant le pic le plus élevé du film après stratification.
  2. Tôle métallique stratifiée pour une boîte de conserve en deux parties selon la revendication 1, dans laquelle une rugosité de surface de ligne centrale Ra d'une surface de la première couche de résine de polyester se situe dans une plage de 0,4 µm à 2,0 µm dans laquelle la rugosité de surface de ligne centrale Ra a été mesurée conformément à la norme JIS-B0601 en utilisant un instrument de mesure de rugosité de surface SE-30D fabriqué par Kosaka Laboratory Ltd. avec une valeur de coupure de 0,8 mm et une longueur de mesure de 2,4 mm, et dans laquelle la mesure a été effectuée en trois points respectifs dans la direction longitudinale et la direction de largeur d'un film, et la valeur moyenne des valeurs Ra a été déterminée comme étant la valeur Ra du film.
  3. Corps de boîte de conserve stratifiée en deux parties fabriqué en utilisant la tôle métallique stratifiée pour une boîte de conserve en deux parties selon la revendication 1 ou 2.
EP13876472.5A 2013-02-28 2013-12-26 Plaque métallique stratifiée pour canettes en deux parties et corps de stratifiée en deux parties Active EP2962951B1 (fr)

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Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201205243D0 (en) 2012-03-26 2012-05-09 Kraft Foods R & D Inc Packaging and method of opening
GB2511560B (en) 2013-03-07 2018-11-14 Mondelez Uk R&D Ltd Improved Packaging and Method of Forming Packaging
GB2511559B (en) 2013-03-07 2018-11-14 Mondelez Uk R&D Ltd Improved Packaging and Method of Forming Packaging
JP6309741B2 (ja) * 2013-11-06 2018-04-11 東洋製罐株式会社 樹脂被覆金属板及びシームレス缶
EP3231723B1 (fr) 2014-12-12 2018-11-28 JFE Steel Corporation Feuille métallique revêtue de résine pour couvercles de boîte
AU2016237966B2 (en) * 2015-03-26 2018-11-22 Jfe Steel Corporation Resin-Coated Metal Sheet for Container
WO2017098818A1 (fr) 2015-12-09 2017-06-15 Ｊｆｅスチール株式会社 Tôle stratifiée pour contenant revêtu de résine à double face
EP3427944B1 (fr) * 2016-03-10 2021-07-14 Nippon Steel Corporation Procede de fabrication d'une plaque metallique filmee ayant une excellente adhesion apres traitement a l'autoclave
CN109071844A (zh) * 2016-04-22 2018-12-21 埃克森美孚化学专利公司 聚乙烯片材
US10815347B2 (en) * 2016-08-11 2020-10-27 Toray Plastics (America), Inc. Blush-resistant film including pigments
US20180104930A1 (en) * 2016-10-17 2018-04-19 Eastman Chemical Company Metal articles with heat laminated clear semi-crystalline polyesters
WO2018221385A1 (fr) * 2017-05-31 2018-12-06 Ｊｆｅスチール株式会社 Plaque métallique revêtue de résine pour récipient
CN109910402B (zh) * 2017-12-13 2021-08-13 宝山钢铁股份有限公司 一种界面气泡率极低的覆膜铁及其制造方法
JP7037108B2 (ja) * 2017-12-15 2022-03-16 東洋紡株式会社 金属板貼合せ成形加工用着色二軸延伸ポリエステルフィルム
JP7195052B2 (ja) * 2018-03-01 2022-12-23 東洋鋼鈑株式会社 容器用樹脂被覆金属板、その樹脂被覆金属板からなる容器、及びその樹脂被覆金属板の製造方法
CN110920167A (zh) * 2018-09-19 2020-03-27 宝山钢铁股份有限公司 一种耐蒸煮变色覆铁膜及其覆膜金属板
MX2022007547A (es) * 2019-12-23 2022-07-19 Jfe Steel Corp Lamina metalica revestida de resina, lata estirada y planchada revestida de resina, y metodo de produccion de lata estirada y planchada revestida de resina.
JP7176668B1 (ja) 2021-03-26 2022-11-22 Ｊｆｅスチール株式会社 容器用樹脂被覆金属板

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5610451A (en) 1979-07-05 1981-02-02 Toray Industries Resin coated metallic plate for vessel
JPH085159B2 (ja) 1988-01-28 1996-01-24 新日本製鐵株式会社 ２層被膜構造を有するラミネート鋼板及びその製造方法
JP2851468B2 (ja) * 1991-12-03 1999-01-27 帝人株式会社 金属板貼合せ成形加工用ポリエステルフィルム
JP3020731B2 (ja) 1992-06-03 2000-03-15 帝人株式会社 金属缶蓋貼合せ被覆透明フィルム
US5900325A (en) * 1993-08-04 1999-05-04 Toyo Kohan Co., Ltd. Polyester laminated metal sheet
JP3343423B2 (ja) * 1993-12-28 2002-11-11 東洋製罐株式会社 絞りしごき缶用樹脂被覆金属板およびこれからなる絞りしごき缶
JP3481196B2 (ja) 2000-09-12 2003-12-22 ユニチカ株式会社 金属板ラミネート用ポリエステルフィルム、ラミネート金属板およびそれを用いた金属容器
JP3753592B2 (ja) 2000-05-30 2006-03-08 ユニチカ株式会社 金属板ラミネート用ポリエステルフィルム
JP2004058402A (ja) 2002-07-26 2004-02-26 Mitsubishi Polyester Film Copp 金属板被覆用フィルム
JP3924239B2 (ja) * 2002-11-20 2007-06-06 新日本製鐵株式会社 容器用金属板およびその製造方法
JP4261253B2 (ja) 2002-12-24 2009-04-30 東洋紡績株式会社 金属板被覆用ポリエステルフィルム、その製造方法およびポリエステルフィルム被覆金属板の製造方法
JP2004345232A (ja) * 2003-05-22 2004-12-09 Jfe Steel Kk 熱処理後の加工性に優れた缶用ラミネート金属板
JP2005161621A (ja) 2003-12-01 2005-06-23 Jfe Steel Kk レトルト後の外観に優れた缶蓋用ラミネート金属板
DK1757439T3 (en) * 2004-05-31 2016-10-17 Jfe Steel Corp Resinbelagt metal plate
JP4825072B2 (ja) * 2005-08-08 2011-11-30 東洋紡績株式会社 金属板ラミネート用フィルム
CN101228233B (zh) 2005-08-08 2012-01-11 东洋纺织株式会社 金属板层叠用薄膜
JP4692144B2 (ja) 2005-08-12 2011-06-01 Ｊｆｅスチール株式会社 ２ピース缶及びその製造方法、並びに２ピース缶用鋼板
US7737246B2 (en) * 2005-12-15 2010-06-15 Eastman Chemical Company Polyester compositions which comprise cyclobutanediol, cyclohexanedimethanol, and ethylene glycol and manufacturing processes therefor
ES2695026T3 (es) * 2006-09-19 2018-12-28 Swimc Llc Recipientes de alimentos y bebidas y métodos de recubrimiento
JP5167846B2 (ja) 2008-02-07 2013-03-21 Ｊｆｅスチール株式会社 ２ピース缶体用ラミネート金属板および２ピースラミネート缶体
JP5347343B2 (ja) * 2008-06-13 2013-11-20 Ｊｆｅスチール株式会社 容器用ポリエステル樹脂被覆金属板
US8800030B2 (en) 2009-09-15 2014-08-05 Symantec Corporation Individualized time-to-live for reputation scores of computer files
MX339459B (es) * 2010-10-15 2016-05-27 Valspar Sourcing Inc Composicion de recubrimiento a base de poliester para sustratos de metal.
EP2752291B1 (fr) 2011-08-31 2023-09-27 JFE Steel Corporation Tôle métallique revêtue de résine
EP2799227B1 (fr) 2011-12-26 2019-03-06 JFE Steel Corporation Feuille stratifiée et boîte de conserve pour aliments
ES2794007T3 (es) 2012-04-19 2020-11-17 Jfe Steel Corp Chapa de metal laminada y recipiente de enlatado para alimentos

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

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WO2014132541A1 (fr) 2014-09-04
MY175366A (en) 2020-06-23
ES2744906T3 (es) 2020-02-26
EP2962951A1 (fr) 2016-01-06
PH12015501883B1 (en) 2015-12-14
CA2901209C (fr) 2017-10-24
EP2962951A4 (fr) 2016-01-06
JP2014166856A (ja) 2014-09-11
US10227156B2 (en) 2019-03-12
CN105008232B (zh) 2019-08-13
BR112015020675A2 (pt) 2017-07-18
TWI549810B (zh) 2016-09-21
JP5874659B2 (ja) 2016-03-02
BR112015020675B1 (pt) 2020-12-08
CA2901209A1 (fr) 2014-09-04
KR20150108905A (ko) 2015-09-30
PH12015501883A1 (en) 2015-12-14
US20160009444A1 (en) 2016-01-14
CN105008232A (zh) 2015-10-28
TW201446486A (zh) 2014-12-16

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